510(k) K885188 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
MODIFIED RT. ARTRIAL AND 13.5X11.5F CATH. TRAY
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Feb 6, 1989 |
| Received | Dec 7, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885188
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.